Variable resistor jaw

ABSTRACT

A bipolar forceps for sealing tissue includes an end effector assembly having opposing first and second jaw members each having a proximal end and a distal end. A first electrically conductive surface having two or more conductive sealing plates and a dielectric layer is operably coupled to the first jaw member. Each sealing plate is connected to a reactive element and positioned along the first electrically conductive surface from the proximal end to the distal end. The reactive element of the sealing plate have different impedances. A second electrically conductive surface having one or more conductive sealing plates is operably coupled to the second jaw member. Each electrically conductive surface on the jaw members connects to a source of electrosurgical energy such that the sealing plates are capable of conducting energy through tissue held therebetween to effect a tissue seal.

CROSS REFERENCE TO RELATED APPLICATIONS

The present application is a Continuation application claiming the benefit of and priority to U.S. patent application Ser. No. 13/922,975, filed on Jun. 20, 2013, which is a continuation of U.S. patent application Ser. No. 12/176,679, filed Jul. 21, 2008, now U.S. Pat. No. 8,469,956. The entire contents of each of the above applications is hereby incorporated by reference.

BACKGROUND

1. Technical Field

The present disclosure relates to electrosurgical forceps for assuring uniform sealing of tissue when performing electrosurgical procedures. More particularly, the present disclosure relates to open or endoscopic bipolar electrosurgical forceps that includes reactive elements for driving different amounts of current through different parts of a jaw member of the forceps in order to get a more controlled distribution of energy along the length of the jaw.

2. Description of the Related Art

Forceps utilize mechanical action to constrict, grasp, dissect and/or clamp tissue. Electrosurgical forceps utilize both mechanical clamping action and electrical energy to effect hemostasis by heating the tissue and blood vessels. By controlling the intensity, frequency and duration of the electrosurgical energy applied through the jaw members to the tissue, the surgeon can coagulate, cauterize and/or seal tissue.

In order to effect a proper seal with larger vessels or thick tissue, many known instruments rely on control of mechanical parameters. Two predominant mechanical parameters that must be accurately controlled are the pressure applied to the tissue and the gap distance between the electrodes. As can be appreciated, both of these parameters are affected by the thickness of vessels or tissue. More particularly, accurate application of pressure is important for several reasons: to reduce the tissue impedance to a low enough value that allows enough electrosurgical energy through the tissue; to overcome the forces of expansion during tissue heating; and to contribute to the end tissue thickness which is an indication of a good seal.

Even with control over mechanical parameters, however, the tissue portion nearest the pivot of the opposing jaw members tend to receive more energy delivery than the portions which are distal thereto. Resistance is expressed as resistivity multiplied by, the length divided by cross-sectional area. The resistance, then, changes as the pressure of the jaws affects the thickness of material held therebetween and the jaw surface area changes. The increased pressure at the distal ends increases both electrical contact and decreases thickness of tissue thereby requiring, in some instances, a greater amount of energy between the distal ends of the opposing jaw members in order to properly and effectively seal larger vessels or tissue. Relying on mechanical parameters alone, without taking into account energy dissipation along the length of the jaw, therefore, can lead to an ineffective seal. Energy distribution, if properly controlled, can assure a consistent and reliable tissue seal by compensating for changes in tissue impedance caused by changes in pressure, surface area, and thickness.

SUMMARY

A bipolar forceps for sealing tissue includes an end effector assembly having opposing first and second jaw members each having a proximal end and a distal end. The jaw members are movable relative to each other in order to grasp tissue therebetween. An electrically conductive surface having two or more conductive sealing plates and a dielectric layer is operably coupled to the first jaw member. Each sealing plate is connected to a reactive element and positioned along the electrically conductive surface from the proximal end to the distal end. The reactive element of the sealing plate positioned on the proximal end of the first jaw member has a different impedance than the reactive element positioned on the distal end. An electrically conductive surface having one or more conductive sealing plates is operably coupled to the second jaw member. Each electrically conductive surface on the jaw members is adapted to be connected to a source of electrosurgical energy such that the sealing plates are capable of conducting energy through tissue held therebetween to effect a tissue seal.

In embodiments, the reactive element is a capacitor, resistor, variable resistor, resistor series, capacitor series, and/or a variable resistor network. In embodiments, the dielectric layer is composed of shape memory materials. In embodiments, the bipolar forceps further includes a sensor for measuring one or more tissue properties. The sensor configures the reactive elements based on one or more tissue properties in order to effectively seal tissue. A feedback loop may be used for real time adjustment of the reactive elements.

The present disclosure also relates to a method of sealing tissue including the steps of: providing a bipolar forceps that includes first and second jaw members each having proximal and distal ends, the first jaw member having an electrically conductive surface having two or more conductive sealing plates and a dielectric disposed therebetween. Each sealing plate is connected to a reactive element and positioned along the electrically conductive surface from the proximal end to the distal end. The reactive element on the proximal end has a higher impedance than the reactive element on the distal end. An electrically conductive surface is included having one or more conductive sealing plates operably coupled to the second jaw member. The method also includes the steps of connecting the jaw members to a source of electrosurgical energy; actuating the jaw members to grasp tissue between opposing jaw members; conducting electrosurgical energy to the electrically conductive surfaces of the jaw members; and controlling the reactive elements of the first jaw member to regulate the electrosurgical energy along the jaw members to effect a tissue seal.

BRIEF DESCRIPTION OF THE DRAWINGS

Various embodiments of the present disclosure are described herein with reference to the drawings wherein:

FIG. 1 is a perspective view of an electrosurgical system including an electrosurgical forceps and an electrical generator in accordance with an embodiment of the present disclosure;

FIG. 2A is a plan view of the electrically conductive surface of a jaw member in accordance with the present disclosure;

FIG. 2B is a perspective view of an embodiment of the jaw members in accordance with the present disclosure;

FIG. 2C is a perspective view of another embodiment of the jaw members in accordance with the present disclosure;

FIG. 2D is a perspective view of yet another embodiment of the jaw members in accordance with the present disclosure;

FIG. 2E is a plan view of another embodiment of the electrically conductive surface of a jaw member in accordance with the present disclosure;

FIG. 2F is a perspective view of one embodiment of the electrically conductive surface of a jaw member including stop members in accordance with the present disclosure;

FIG. 2G is a side view of one embodiment of the electrically conductive surface of a jaw member including a dielectric layer of varying width in accordance with the present disclosure;

FIG. 3 is a schematic electrical diagram of the end effector assembly and generator of the electrosurgical forceps of FIG. 1;

FIG. 4 is a schematic electrical diagram of another embodiment of the end effector assembly and generator in accordance with the present disclosure;

FIG. 5 is a schematic electrical diagram of another embodiment of the end effector assembly and generator in accordance with the present disclosure;

FIG. 6 is a schematic electrical diagram of another embodiment of the end effector assembly and generator with the resistors arranged in series in accordance with the present disclosure;

FIG. 7 is a schematic electrical diagram of another embodiment of the end effector assembly and generator of the electrosurgical forceps; and

FIG. 8 is a schematic electrical diagram of a variable resistor which may be used with the electrosurgical forceps in accordance with the present disclosure.

FIG. 9 is a schematic electrical diagram of an end effector assembly and generator having a shape memory switch.

DETAILED DESCRIPTION

Various embodiments of the present disclosure are described hereinbelow with reference to the accompanying drawings. Well-known functions or constructions are not described in detail to avoid obscuring the present disclosure in unnecessary detail. Those skilled in the art will understand that the present disclosure may be adapted for use with either an endoscopic instrument or an open instrument; however, different electrical and mechanical connections and considerations apply to each particular type of instrument. The novel aspects with respect to vessel and tissue sealing are generally consistent with respect to both the open and endoscopic designs. In the drawings and in the description which follows, the term “proximal”, as is traditional, will refer to the end of the forceps which is closer to the user, while the term “distal” will refer to the end of the forceps which is further from the user.

Referring now to FIG. 1, a bipolar electrosurgical system according to the present disclosure is shown including electrosurgical forceps 10 configured to support end effector assembly 100. Forceps 10 typically includes various conventional features (e.g., a housing 60, a handle assembly 74, a rotating assembly 80, a trigger assembly 70, etc.) that enable forceps 10 and end effector assembly 100 to mutually cooperate to grasp, seal and, if warranted, divide tissue. Forceps 10 generally includes housing 60 and handle assembly 74 that includes moveable handle 62 and handle 72 which is integral with housing 60. Handle 62 is moveable relative to handle 72 to actuate end effector assembly 100 to grasp and treat tissue. Forceps 10 also includes shaft 64 that has distal end 68 that mechanically engages end effector assembly 100 and proximal end 69 that mechanically engages housing 60 proximate rotating assembly 80 disposed at the distal end of housing 60. Rotating assembly 80 is mechanically associated with shaft 64. Movement of rotating assembly 80 imparts similar rotational movement to shaft 64 which, in turn, rotates end effector assembly 100.

End effector assembly 100 includes two jaw members 110 and 120 having proximal ends 111, 121 and distal ends 113, 123. Jaw members 110 and 120 are movable from a first position wherein jaw members 110 and 120 are spaced relative to another, to a second position wherein jaw members 110 and 120 are closed and cooperate to grasp tissue therebetween. Each jaw member 110 and 120 includes electrically conductive surface 112 and 122, respectively, disposed on an inner-facing surface thereof. Electrically conductive surfaces 112 and 122 cooperate to seal tissue held therebetween upon the application of electrosurgical energy. Electrically conductive surfaces 112 and 122 are connected to generator 20 that communicates electrosurgical energy through the tissue held therebetween. A dielectric layer, or insulator substance, 114 may be included to limit and/or reduce many of the known undesirable effects related to tissue sealing, e.g., flashover, thermal spread and stray current dissipation. By controlling the intensity, frequency and duration of the electrosurgical energy applied to tissue, the tissue can be selectively sealed.

Generator 20 includes a plurality of outputs for interfacing with various electrosurgical instruments (e.g., a monopolar active electrode, return electrode, bipolar electrosurgical forceps, footswitch, etc.). Further, generator 20 includes electronic circuitry configured for generating radio frequency power specifically suited for sealing tissue.

Forceps 10 are connected to a source of electrosurgical energy, e.g., electrosurgical generator 20, via one or more electrical cables. Electrically conductive surfaces 112 and 122, that act as active and return electrodes, are connected to the generator 20 through cable 23, which includes the supply and return lines coupled to active and return terminals 30, 32. Electrosurgical forceps 10 is coupled to generator 20 at active and return terminals 30 and 32 (e.g., pins) via plug 92 disposed at the end of cable 23, wherein plug 92 includes contacts from the supply and return lines. Electrosurgical RF energy is supplied to forceps 10 by generator 20 via a supply line connected to the active electrode and returned through a return line connected to the return electrode.

Generator 20 includes suitable input controls 25 (e.g., buttons, activators, switches, touch screen, etc.) for controlling the generator 20. In addition, generator 20 includes one or more display screens 27 for providing the surgeon with variety of output information (e.g., intensity settings, treatment complete indicators, etc.). The controls allow the surgeon to adjust power of the RF energy, waveform, and other parameters to achieve the desired waveform suitable for a particular task (e.g., coagulating, tissue sealing, division with hemostatis, etc.). Further, forceps 10 may include a plurality of input controls which may be redundant with certain input controls 25 of generator 20. Placing the input controls at forceps 10 allows for easier and faster modification of RF energy parameters during the surgical procedure without requiring interaction with generator 20.

When the electrosurgical energy is transferred to the end effector assembly 100, a sensor, schematically illustrated as 117, may be employed to determine pre-surgical, concurrent surgical (i.e., during surgery), and/or post-surgical conditions. The sensor 117 may be any of a variety of sensors, such as, for example, a thickness sensor, optical sensor, or proximal sensor. The sensor 117 may measure tissue properties such as tissue thickness, tissue hydration level, tissue impedance, tissue density, tissue type, and other tissue properties as within the purview of those skilled in the art. The sensor 117 may also measure standard electrical parameters such as voltage, current, impedance, and phase. The sensor 117 may be utilized with a closed-loop feedback system coupled to the electrosurgical generator to regulate the electrosurgical energy based upon one or more pre-surgical, concurrent surgical, or post surgical conditions. The feedback loop provides real-time adjustment of the reactive elements based on the tissue property being measured. It is also contemplated that forceps 10 and/or electrosurgical generator 20 used in connection with forceps 10 may include a sensor 117 or feedback mechanism which automatically selects the appropriate amount of electrosurgical energy to effectively seal the particularly-sized tissue grasped between jaw members 110 and 120. The sensor 117 or feedback mechanism may also measure the impedance across the tissue during sealing and provide an indicator (visual and/or audible) that an effective seal has been created between jaw members 110 and 120. Various sensor mechanisms and feedback systems are described in commonly-owned, co-pending U.S. patent application Ser. No. 10/427,832 entitled “METHOD AND SYSTEM FOR CONTROLLING OUTPUT OF RF MEDICAL GENERATOR” filed on May 1, 2003.

Other electrical connections are positioned through shaft 64 and end effector assembly 100 to supply bipolar electrical energy to opposing electrically conductive surfaces 112 and 122 of jaw members 110 and 120, respectively. Forceps 10 also includes a drive assembly (not shown) which imparts movement of jaw members 110 and 120 from the open position to the clamping or closed position. When electrically conductive surfaces 112 and 122 of jaw members 110 and 120 are fully compressed about the tissue, forceps 10 is ready for selective application of electrosurgical energy.

The details relating to the inter-cooperative relationships of the inner-working components of forceps 10 are disclosed in commonly-owned U.S. patent application Ser. No. 11/348,072. Mechanical and cooperative relationships with respect to the various moving elements of handle assembly 74, rotating assembly 80, and end effector assembly 100 are further described by example with respect to commonly-owned U.S. patent application Ser. Nos. 10/369,894 and 10/460,926.

Referring now to FIG. 2A, a plan view of electrically conductive surface 112 of jaw member 110 is shown. First jaw member 110 includes one or more sealing plates 116 on electrically conductive surfaces 112. Sealing plates 116 a, 116 b, and 116 c are positioned along electrically conducting surface 112 from proximal end 111 to distal end 113. Sealing plates 116 a, 116 b, and 116 c each include at least one reactive element for effecting the tissue seal. Reactive elements may include a capacitor, resistor, variable resistor, resistor series, capacitor series, and/or variable resistor network as will be described in detail below.

As illustrated in FIGS. 2B-2D, different embodiments are envisioned for altering the impedance at different locations about first jaw member 110. As shown in FIG. 2B, first jaw member 110 includes sealing plates 116 a, 116 b, and 116 c disposed about dielectric 114. FIG. 2C illustrates first jaw member 110 including sealing plates 116 a, 116 b, 116 c, and 116 d placed proximal to dielectric 114 which is proximal to electrically conductive sealing surface 112 which is composed of electrically isolated sections 112 a, 112 b, 112 c, and 112 d having substantially the same geometry as the sealing plates. FIG. 2D illustrates seal plate 116 having a variable width along the length of jaw member 110 proximal to dielectric 114. Single sealing plate 116 provides a smooth change in capacitance along the length of the jaw. Slotted electrically conductive surface 112 allows each electrically isolated section 112 a, 112 b, 112 c, 112 d, and 112 e to couple to sealing plate 116 independently and spread current.

Sealing plates 116 may be arranged in any configuration conducive to effectively seal tissue as understood by those skilled in the art. Further, the jaw member may have any number of seal plates in any design, such as the jaw member illustrated in FIG. 2E. Sealing plates 116 may be composed of metal, such as surgical stainless steel, or other conducting materials, such as, for example, carbon. Non-conducting material 114 may be an insulating material, such as, for example, polymers including, but not limited to, polyethylene, polytetrafluoroethylene, ethylene propylene diene monomer rubber, and the like. In a like manner, second jaw member 120 may also have a similar construction as jaw member 110 described above and include one or more sealing plates.

In embodiments, at least one stop member 115, as illustrated in FIG. 2F, may be disposed on the inner facing surfaces of electrically conductive sealing surface 112 or 122 to facilitate gripping and manipulation of tissue and to define a gap between opposing jaw members 110 and 120 during sealing and/or cutting of tissue. Stop member 115 may extend from the sealing surface 122 a predetermined distance according to the specific material properties (e.g., compressive strength, thermal expansion, etc.) to yield a consistent and accurate gap distance during sealing. In embodiments, the gap distance between opposing sealing surfaces 112 and 122 during sealing ranges from about 0.001 inches to about 0.006 inches, in other embodiments, from about 0.002 and about 0.003 inches. The non-conductive stop members 115 may be part of dielectric layer 114. Stop member 115 may also be molded onto jaw members 110 and 120 (e.g., overmolding, injection molding, etc.), stamped onto the jaw members 110 and 120, or deposited (e.g., deposition) onto the jaw members 110 and 120. For example, one technique involves thermally spraying a ceramic material onto the surface of jaw members 110 and 120 to form stop members 115. Several thermal spraying techniques are contemplated which involve depositing a broad range of heat resistant and insulative materials on various surfaces to create stop members 115 for controlling the gap distance between electrically conductive surfaces 112 and 122.

It is envisioned that a series of stop members 115 may be employed on one or both jaw members 110 and 120 during sealing and/or cutting of tissue. The series of stop members 115 may be employed on one or both jaw members 110 and 120 depending upon a particular purpose or to achieve a desired result. A detailed discussion of these and other envisioned stop members 115 as well as various manufacturing and assembly processes for attaching and/or affixing stop members 115 to the electrically conductive sealing surfaces 112, 122 are described in commonly-assigned, co-pending U.S. Application Serial No. PCT/US01/11413 entitled “VESSEL SEALER AND DIVIDER WITH NON-CONDUCTIVE STOP MEMBERS” by Dycus et al.

FIG. 3 illustrates a schematic diagram of end effector assembly 100 and generator 20. Generator 20 provides a source voltage, V_(S), to jaw members 110 and 120. Disposed between conductive sealing plates 116 and 126 of jaw members 110 and 120 is a dielectric, or non-conducting layer, 114, thereby forming a capacitor when compressed on tissue having a capacitance between each of the sealing plates 116 (e.g., C₁ and C₂).

The width and thickness of dielectric layer 114 and the surface area of plates 116 a, 116 b, and 116 c may be adjusted to achieve specific capacitances, which represent a specific impedance to RF generator 20. Dielectric layer 114 may have a varying thickness across the surface thereof, such that, for example, dielectric layer 114 is of one thickness around plate 116 a, another thickness around plate 116 b, and yet another thickness around plate 116 c, as illustrated in FIG. 2G. In embodiments, the dielectric layer 114 may be of varying thickness or material composition across conducting surface 112 or each plate 116, e.g. the carbon amount in filled ethylene propylene diene monomer rubber (EPDM) may be varied along the length of jaw members 110 and 120.

Capacitance and area are calculated based on standard capacitance formula:

${C\left( {E_{R},A,d} \right)} = \frac{E_{O} \cdot E_{R} \cdot A}{d}$ ${A_{C}\left( {C,E_{R},d} \right)} = \frac{C \cdot d}{E_{O} \cdot E_{R}}$

wherein: EO is the absolute permittivity=8.854*10-12 Farad/meter (F/m), ER is the relative permittivity of the insulation material in (F/m), A is the surface area of the jaws in meters squared (m2), and d is the distance between the jaws in meters (m).

The relative permittivity, ER, varies with substance or material selection, examples of which are given in Table 1:

TABLE 1 Material Relative Permittivity (F/m) Air 1.0 Polythene/Polyethylene 2.3 PTFE 2.1 Silicone Rubber 3.1 FR4 Fiberglass 4.5 PVC 5.0

The formula to calculate the impedance of a capacitor at the specified frequency C in hertz, is in Farads F:

${R_{C}\left( {C,F} \right)} = \frac{1}{2 \cdot \pi \cdot F \cdot C}$ ${C_{R}\left( {R,F} \right)} = \frac{1}{2 \cdot \pi \cdot F \cdot R}$

For example, assuming that capacitances, C₁=500 ohms and C₂=1000 ohms, are desired at 472 Khz, and a high dielectric with a relative permittivity of 5.0 (ER=5.0) and a thickness of 0.5 mm is used. The sealing plate areas needed are calculated as follow:

ER=5.0 d=0.5×10-3 r=500 f=470×10-3

AC(Cr(r,f),ER,d)=7.649×10-3 m

ER=5.0 d=0.5×10-3 r=500 f=470×10-3

AC(Cr(r,f),ER,d)=3.825×10-3 m

Taking the square root of the area derived, to create a capacitor of equivalent impedance of 500 ohms at 472 Khz, a sealing plate of 2.77 mm² is required. For the 1000 ohm impedance, a sealing plate of 2 mm² would be used.

By specifically designing the plates 116 and dielectric layer 114 to have a certain capacitive impedance, the circuit of FIG. 4 can be established. Generator 20 generates a source voltage, V_(S). First jaw 110 includes three sealing plates 116 a, 116 b, and 116 c separated from sealing plate 126 of second jaw member 120 via dielectric 114. Source voltage V_(S) is constant and is applied across all three plates 116 a, 116 b, and 116 c. Plates 116 a and 116 b, however, include parallel reactive elements R_(a) and R_(b), respectively. R_(a) has a greater resistance than R_(b) such that with application of a constant voltage, the impedance to the tissue through plates 116 a, 116 b, and 116 c increase towards the proximal end of jaw members 110 and 120 thereby driving more current through distal end 111. In FIG. 4 and other embodiments described herein, the reactive elements, R, may be any of capacitors, resistors, variable resistors, resistor series, capacitor series, and/or variable resistor networks to provide the impedance needed to control current through the jaws and is therefore not limited to the particular reactive element exemplified in the embodiments.

End effector assembly 100 may be constructed as shown, or in reverse, so that jaw member 120 includes more than one plate and associated reactive element. In embodiments, such as that shown in FIG. 5, jaw member 110 can be split into proximal and distal plates, 116 a and 116 b, connected by the same wire from voltage source, V_(S), but with increased impedance between the wire and the proximal end by use of reactive element R_(a) which is greater than R_(b).

In yet other embodiments, such as that shown in FIG. 6, resistors R_(a), R_(b), R_(c), and R_(d) are connected in series across voltage source V_(S) thereby forming a voltage divider. The voltage divider may consist of any two or more resistors connected in series across voltage source 20. Resistors R_(a), R_(b), R_(c), and R_(d) decrease in resistance along the length of jaw member 110 towards distal end 113. The source voltage V_(S) must be as high as or higher than any voltage developed by the voltage divider. As the source voltage is dropped in successive steps through the series resistors, the source voltage is tapped off to supply individual voltage requirements to each plate 116. The values of the series resistors used are determined by the voltage and current requirements of plates 116 a, 116 b, and 116 c as explained above.

In other embodiments, any number of plates may be used with any number of resistors in any of the configurations described above, such as, for example, as illustrated in FIG. 7.

In other embodiments, variable resistors may be used. Variable resistor, R_(V), such as that shown in FIG. 8, allows adjustment of the resistance between two points, 132 and 134, in the circuit via spindle 136. It is useful for setting the value of the resistor while in use depending on changes in other parameters, such as, for example, the distance between plates 116, 126.

It is also envisioned that the dielectric 114 may be made of a material that expands with temperature, such as shape memory alloys or polymers. Shape memory alloys (SMAs) are a family of alloys having anthropomorphic qualities of memory and trainability and are particularly well suited for use with medical instruments. One of the most common SMAs is Nitinol which can retain shape memories for two different physical configurations and changes shape as a function of temperature. Recently, other SMAs have been developed based on copper, zinc and aluminum and have similar shape memory retaining features.

SMAs undergo a crystalline phase transition upon applied temperature and/or stress variations. A particularly useful attribute of SMAs is that after it is deformed by temperature/stress, it can completely recover its original shape on being returned to the original temperature. The ability of an alloy to possess shape memory is a result of the fact that the alloy undergoes a reversible transformation from an austenite state to a martensite state with a change in temperature (or stress-induced condition). This transformation is referred to as a thermoelastic martensite transformation.

Under normal conditions, the thermoelastic martensite transformation occurs over a temperature range which varies with the composition of the alloy, itself, and the type of thermal-mechanical processing by which it was manufactured. In other words, the temperature at which a shape is “memorized” by an SMA is a function of the temperature at which the martensite and austenite crystals form in that particular alloy. For example, Nitinol alloys can be fabricated so that the shape memory effect will occur over a wide range of temperatures, e.g., −270° to +100° Celsius.

Shape memory polymers (SMPs) may be used instead of, or may augment the use of, SMAs. SMPs are generally characterized as phase segregated linear block co-polymers having a hard segment and a soft segment. The hard segment is typically crystalline, with a defined melting point, and the soft segment is typically amorphous, with a defined glass transition temperature. In embodiments, however, the hard segment may be amorphous and have a glass transition temperature and the soft segment may be crystalline and have a melting point. The melting point or glass transition temperature of the soft segment is substantially less than the melting point or glass transition temperature of the hard segment.

When the SMP is heated above the melting point of the hard segment the material can be shaped. This shape can be memorized by cooling the SMP below the melting point of the hard segment. When the shaped SMP is cooled below the glass transition temperature of the soft segment while the shape is deformed, a new temporary shape can be set. The original shape can be recovered by heating the material above the glass transition temperature of the soft segment but below the melting point of the hard segment. The recovery of the original shape, which is induced by an increase in temperature, is called the thermal shape memory effect.

Because capacitance is proportional to the dielectric constant and to the surface area of the plates and inversely proportional to the distance between the plates, a dielectric composed of shape memory material that expands with temperature will result in decreased capacitance and increased jaw impedance. Thus, a jaw constructed of shape memory materials will impede RF as the temperature rises.

It is also envisioned, as illustrated in FIG. 9, that a switch may be utilized with the embodiments of the present disclosure. Switch 140 may be composed of a shape memory material to detect a change in temperature of current. Switch 140 establishes contact with a corresponding electrical contact when a particular temperature is reached to allow current to flow therethrough.

While several embodiments of the disclosure have been shown in the drawings and/or discussed herein, it is not intended that the disclosure be limited thereto, as it is intended that the disclosure be as broad in scope as the art will allow and that the specification be read likewise. Therefore, the above description should not be construed as limiting, but merely as exemplifications of particular embodiments. Those skilled in the art will envision other modifications within the scope and spirit of the claims appended hereto. 

1-18. (canceled)
 19. A bipolar forceps for sealing tissue, comprising: an end effector assembly having opposing first and second jaw members each having a proximal end and a distal end, at least one of the first and second jaw members movable relative to the other one from a first position wherein the first and second jaw members are spaced apart from one another to a second position for grasping tissue therebetween, the first jaw member including: a first electrically conductive surface including a first electrically isolated section and a second electrically isolated section positioned proximal to the first electrically isolated section; a first sealing plate disposed adjacent the first electrically isolated section electrically coupled to an electrosurgical energy source; a second sealing plate disposed adjacent the second electrically isolated section electrically coupled to the electrosurgical energy source; and a non-conducting layer disposed between the first electrically conductive surface and the first sealing plate and disposed between the first electrically conductive surface and the second sealing plate; the second jaw member including a second electrically conductive surface opposing the first electrically conductive surface, wherein impedance is varied between the first and second electrically conductive surfaces and grasped tissue from the proximal end of the first and second electrically conductive surfaces to the distal end of the first and second electrical conductive surfaces during electrical activation of the electrosurgical energy source.
 20. The bipolar forceps according to claim 19, wherein the impedance between the first and second electrically conductive surfaces and grasped tissue is increases toward the proximal end of the end effector assembly.
 21. The bipolar forceps according to claim 19, wherein the first sealing plate has the same geometry of the first electrically isolated section and the second sealing plate has the same geometry of the second electrically isolated section.
 22. The bipolar forceps according to claim 19, wherein the non-conducting layer varies in thickness along the length of the first jaw member.
 23. The bipolar forceps according to claim 19, wherein at least one of the first electrically conductive surface or the second electrically conductive surface includes stop members that regulate the distance between first and second jaw members.
 24. The bipolar forceps according to claim 19, further comprising a sensor disposed on one of the first or second jaw members positioned to measure at least one tissue property and to relay the measured at least one tissue property to the source of electrosurgical energy to effectively seal tissue.
 25. The bipolar forceps according to claim 24, wherein the at least one tissue property measured by the sensor includes at least one of tissue thickness, tissue hydration level, tissue impedance, tissue density, tissue type, voltage, current, impedance, or phase.
 26. The bipolar forceps according to claim 24, further comprising a feedback loop that provides real time adjustment of the electrosurgical energy source based on the at least one tissue property.
 27. The bipolar forceps according to claim 19, wherein each of the first and second sealing plates includes a reactive element for effecting a tissue seal of the grasped tissue.
 28. The bipolar forceps according to claim 27, wherein the reactive element may be selected from the group consisting of a capacitor, resistor, variable resistor, resistor series, capacitor series, variable resistor network, and/or combinations thereof.
 29. A bipolar forceps for sealing tissue, comprising: an end effector assembly having opposing first and second jaw members each having a proximal end and a distal end, at least one of the first and second jaw members movable relative to the other one from a first position wherein the first and second jaw members are spaced apart from one another to a second position for grasping tissue therebetween, the first jaw member including: a first electrically conductive surface including a plurality of electrically isolated sections positioned from the proximal end to the distal end of the first electrically conductive surface; a plurality of sealing plates with each sealing plate of the plurality of sealing plates disposed adjacent a respective electrically isolated section of the plurality of electrically isolated section, each sealing plate of the plurality of sealing plates electrically coupled to an electrosurgical energy source; and a non-conducting layer disposed between the first electrically conductive surface and the plurality of sealing plates; the second jaw member including a second electrically conductive surface opposing the first electrically conductive surface, wherein impedance is varied between the first and second electrically conductive surfaces and grasped tissue from the proximal end of the first and second electrically conductive surfaces to the distal end of the first and second electrical conductive surfaces during electrical activation of the electrosurgical energy source.
 30. The bipolar forceps according to claim 29, wherein impedance between each electrically isolated section of the plurality of electrically isolated section and grasped tissue increases toward the proximal end of the end effector assembly.
 31. The bipolar forceps according to claim 29, further comprising a feedback loop that provides real time adjustment of the electrosurgical energy source based on the at least one tissue property.
 32. The bipolar forceps according to claim 29, wherein the non-conducting layer varies in thickness along the length of the first jaw member.
 33. The bipolar forceps according to claim 29, wherein the first electrically conductive surface includes stop members that regulate the distance between the first and second jaw members.
 34. The bipolar forceps according to claim 29, wherein the non-conductive layer includes stop members that regulate the distance between the first and second jaw members.
 35. An end effector assembly, comprising: a first jaw member having a proximal and distal end and including: a first electrically conductive surface including a first electrically isolated section and a second electrically isolated section positioned proximal to the first electrically isolated section; a first sealing plate disposed adjacent the first electrically isolated section electrically coupled to an electrosurgical energy source; a second sealing plate disposed adjacent the second electrically isolated section electrically coupled to the electrosurgical energy source; and a non-conducting layer disposed between the first electrically conductive surface and the first sealing plate and disposed between the first electrically conductive surface and the second sealing plate; a second jaw member having a proximal and distal end and including a second electrically conductive surface opposing the first electrically conductive surface, wherein the first and second jaw members are movable relative to one another from a first position wherein the first and second jaw members are spaced apart from one another to a second position for grasping tissue therebetween, and wherein impedance is varied between the first and second electrically conductive surfaces and grasped tissue from the proximal end of the first and second electrically conductive surfaces to the distal end of the first and second electrical conductive surfaces during electrical activation of the electrosurgical energy source. 